GB0221207D0 - Method of reacting carboxylic acids - Google Patents

Method of reacting carboxylic acids

Info

Publication number
GB0221207D0
GB0221207D0 GBGB0221207.4A GB0221207A GB0221207D0 GB 0221207 D0 GB0221207 D0 GB 0221207D0 GB 0221207 A GB0221207 A GB 0221207A GB 0221207 D0 GB0221207 D0 GB 0221207D0
Authority
GB
United Kingdom
Prior art keywords
carboxylic acid
channel
liquid
electrical voltage
acid molecules
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GBGB0221207.4A
Other versions
GB2392920B (en
GB2392920A (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University of Hull
Original Assignee
University of Hull
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by University of Hull filed Critical University of Hull
Priority to GB0221207A priority Critical patent/GB2392920B/en
Publication of GB0221207D0 publication Critical patent/GB0221207D0/en
Priority to AT03255348T priority patent/ATE358736T1/en
Priority to DE60312936T priority patent/DE60312936T2/en
Priority to EP03255348A priority patent/EP1398396B1/en
Priority to US10/659,738 priority patent/US7279082B2/en
Publication of GB2392920A publication Critical patent/GB2392920A/en
Application granted granted Critical
Publication of GB2392920B publication Critical patent/GB2392920B/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0093—Microreactors, e.g. miniaturised or microfabricated reactors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
    • C07C1/207—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
    • C07C1/207—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds
    • C07C1/2078—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds by a transformation in which at least one -C(=O)-O- moiety is eliminated
    • C25B3/10—
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/20—Processes
    • C25B3/29—Coupling reactions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781—Aspects relating to microreactors
    • B01J2219/00783—Laminate assemblies, i.e. the reactor comprising a stack of plates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781—Aspects relating to microreactors
    • B01J2219/00819—Materials of construction
    • B01J2219/00824—Ceramic
    • B01J2219/00826—Quartz
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781—Aspects relating to microreactors
    • B01J2219/00851—Additional features
    • B01J2219/00853—Employing electrode arrangements

Abstract

Electrical voltage is applied between ends of a channel containing a liquid and carboxylic acid molecules (I,II) having carbon atom alpha to carboxylic acid group are supplied to channel. Electrical voltage makes carboxylic acid molecules to react, carboxylic acid groups are lost, and product molecule is formed in which alpha carbons are bonded. The reaction takes place in liquid in the channel and spaced from electrodes. Electrical voltage is applied between opposite ends of a channel containing a liquid using electrodes and carboxylic acid molecules (I,II) having carbon atom alpha to carboxylic acid group are supplied to the channel. The electrical voltage makes the carboxylic acid molecules to react with the loss of carboxylic acid groups. A product molecule is formed in which alpha carbons are bonded. The reaction takes place in the liquid in the channel and spaced from the electrodes. Carboxylic acids are thus reacted.
GB0221207A 2002-09-12 2002-09-12 Method of reacting carboxylic acids Expired - Fee Related GB2392920B (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
GB0221207A GB2392920B (en) 2002-09-12 2002-09-12 Method of reacting carboxylic acids
AT03255348T ATE358736T1 (en) 2002-09-12 2003-08-28 METHOD OF ALLOWING CARBOXYLIC ACIDS TO REACT
DE60312936T DE60312936T2 (en) 2002-09-12 2003-08-28 Method for reacting carboxylic acids
EP03255348A EP1398396B1 (en) 2002-09-12 2003-08-28 Method of reacting carboxylic acids
US10/659,738 US7279082B2 (en) 2002-09-12 2003-09-11 Method of reacting carboxylic acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB0221207A GB2392920B (en) 2002-09-12 2002-09-12 Method of reacting carboxylic acids

Publications (3)

Publication Number Publication Date
GB0221207D0 true GB0221207D0 (en) 2002-10-23
GB2392920A GB2392920A (en) 2004-03-17
GB2392920B GB2392920B (en) 2006-03-08

Family

ID=9943968

Family Applications (1)

Application Number Title Priority Date Filing Date
GB0221207A Expired - Fee Related GB2392920B (en) 2002-09-12 2002-09-12 Method of reacting carboxylic acids

Country Status (5)

Country Link
US (1) US7279082B2 (en)
EP (1) EP1398396B1 (en)
AT (1) ATE358736T1 (en)
DE (1) DE60312936T2 (en)
GB (1) GB2392920B (en)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1443445A1 (en) * 1962-08-04 1968-11-21 Walter Bloechl Process for the preparation of mono- and difunctional fluoroalkane derivatives
DE1643693B2 (en) * 1967-11-11 1976-09-09 Basf Ag, 6700 Ludwigshafen PROCESS FOR THE PREPARATION OF SEBACIC ACID DIMETHYLESTER BY ELECTROLYTIC CONDENSATION OF ADIPIC ACID MONOMETHYLESTER
US4006065A (en) * 1972-06-26 1977-02-01 Otto Meresz Process for the synthesis of pure isomers of long chain alkenes
DE4221555A1 (en) * 1992-07-01 1994-01-05 Hoechst Ag Process for the preparation of perfluoropolyethers
US6238543B1 (en) * 1997-10-17 2001-05-29 E. I. Du Pont De Nemours And Company Kolbe electrolysis in a polymer electrolyte membrane reactor
GB2379018B (en) * 2001-08-10 2006-02-22 Univ Hull Monitoring of chemical reactions

Also Published As

Publication number Publication date
EP1398396B1 (en) 2007-04-04
US7279082B2 (en) 2007-10-09
EP1398396A1 (en) 2004-03-17
DE60312936D1 (en) 2007-05-16
GB2392920B (en) 2006-03-08
ATE358736T1 (en) 2007-04-15
US20040079630A1 (en) 2004-04-29
DE60312936T2 (en) 2007-08-30
GB2392920A (en) 2004-03-17

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Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee

Effective date: 20080912